On September 25, 2024, the Food Standards Agency (FSA) and Food Standards Scotland (FSS) issued important guidance on caffeine in food supplements. This new guidance aims to promote safe consumption and manufacturing practices for supplements containing high levels of caffeine.

Marketing medical devices can be a challenge. The Advertising Standards Authority (ASA) and Committee of Advertising Practice (CAP) shape the rules for advertising in the UK, including what you can and cannot say about medical devices.

Since Brexit, importing goods into Great Britain has completely changed bringing with it a labyrinth of new regulations and standards impacting the smooth operation of businesses dealing in dietary supplements, food supplement, vitamins, and other nutrition-focused products.

Labelling cosmetic products is an essential part of product compliance. The UK has strict regulations so understanding the nuances of when it comes to creating labels for your cosmetics is really important.

Medical device registrations and regulations are ever evolving so understanding how a UKRP can help has become a really important part of post-Brexit processes.

The UK's regulatory environment for medical devices has evolved over the years. Historically, we followed the European Union's Medical Device Directive (MDD). However, post-Brexit, we have established our own regulatory system.

In the bustling world of health and wellness, food supplements have become an integral part of many individuals' daily routines. Whether it's bolstering essential nutrients or supporting specific health goals, the demand for these products continues to soar.

In the landscape of consumer safety and regulatory compliance, the UK Responsible Person plays a pivotal role in ensuring that products placed on the market meet the necessary standards and requirements.

It's with immense joy and gratitude that Taylored Consultancy celebrates 1 year in business. What a remarkable journey it has been!